Rock Crystal, Apicella Alfonso Junior
Department of Biology, Neuroscience Institute, University of Texas at San Antonio, San Antonio, Texas 78249.
Department of Biology, Neuroscience Institute, University of Texas at San Antonio, San Antonio, Texas 78249
J Neurosci. 2015 Apr 29;35(17):6703-13. doi: 10.1523/JNEUROSCI.5049-14.2015.
In the auditory cortex (AC), interhemispheric communication is involved in sound localization processes underlying spatial hearing. However, the neuronal microcircuits recruited by the callosal projections are unknown. We addressed this fundamental question by taking advantage of optogenetics and examining directly the functional effects of interhemispheric inputs to specific pyramidal neurons in layer 5 of the mouse AC, defined by their output as either corticocortical (CCort) or corticocollicular (CCol). We found that callosal projections suppress the activity of CCort pyramidal neurons, but facilitate firing of CCol pyramidal neurons. This difference is mechanistically explained by callosal activation of fast-spiking parvalbumin-expressing interneurons (FS-PARV), which provide selective inhibition to CCort pyramidal neurons. Our results establish two distinct previously unknown cortical circuits underlying either callosal suppression (callosal projections → FS-PARV → CCort) or facilitation (callosal projections → CCol) of projecting neurons in layer 5 of the AC and attribute a specific function to a genetically defined type of interneuron in interhemispheric communication.
在听觉皮层(AC)中,半球间通讯参与空间听觉的声音定位过程。然而,胼胝体投射所招募的神经元微回路尚不清楚。我们利用光遗传学技术,直接检测了小鼠AC第5层特定锥体神经元的半球间输入的功能效应,以此解决了这个基本问题,这些锥体神经元根据其输出分为皮质-皮质(CCort)或皮质-丘系(CCol)。我们发现,胼胝体投射抑制CCort锥体神经元的活动,但促进CCol锥体神经元的放电。这种差异在机制上是由表达小白蛋白的快速放电中间神经元(FS-PARV)的胼胝体激活所解释的,FS-PARV对CCort锥体神经元提供选择性抑制。我们的研究结果建立了两个不同的、先前未知的皮层回路,分别负责AC第5层投射神经元的胼胝体抑制(胼胝体投射→FS-PARV→CCort)或促进(胼胝体投射→CCol),并赋予了一种基因定义的中间神经元类型在半球间通讯中的特定功能。